HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56041552T= , CM000674.2:g.56041552T= | GRCh38 |
NC_000012.11:g.56435336T= , CM000674.1:g.56435336T= | GRCh37 |
NC_000012.10:g.54721603T= | NCBI36 |
NG_023201.1:g.4651T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356464.10:c.-357+156T= | ENSP00000348849.5:n.-357+156T= | |
XR_944989.1:n.161A= | ||
XR_944990.1:n.161A= | ||
XR_944989.3:n.452A= | ||
XR_944990.3:n.452A= |